Sergey Cheskis
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Sergey Cheskis has a total of 16 co-authors. Here are the top co-authors by number of shared publications:
- Igor Rahinov
Department of Natural Sciences, The Open University of Israel, 4353701 Raanana, Israel
5 shared publications Alexey Fomin
Tel Aviv University
3 shared publicationsVladimir Tsionsky
Tel Aviv University
3 shared publicationsMarina Poliak
School of Chemistry, Tel Aviv University, Tel Aviv 69978, Israel
2 shared publicationsAlexander Kachanov
Laboratoire de Spectrométrie Physique, CNRS (UM5588), Université Joseph Fourier, Grenoble I, B.P.87, 38402, Saint-Martin-d'Hères Cedex, France
1 shared publicationAnita Pilipodi Best
Tel Aviv University
1 shared publication
Latest Publications
- Open Access
- 30 September 2026
- Published by Elsevier in Proceedings of the Combustion Institute
- Vol. 42
Role of early particle formation in modeling gas-phase chemistry of Fe-doped flames
- 30 September 2026
- Published by Elsevier in Proceedings of the Combustion Institute
- Vol. 42
Open AccessRole of early particle formation in modeling gas-phase chemistry of Fe-doped flames
- 28 July 2018
- Published by Springer Nature in Applied Physics B
- Vol. 124 (8) , 164
Concentration measurements by intracavity laser absorption spectroscopy for the case of strongly overlapped spectra
- 28 July 2018
- Published by Springer Nature in Applied Physics B
- Vol. 124 (8) , 164
Concentration measurements by intracavity laser absorption spectroscopy for the case of strongly overlapped spectra
- 1 October 2013
- Published by Elsevier in Combustion and Flame
- Vol. 160 (10) , 2131-2140
Combined particle mass spectrometer – Quartz crystal microbalance apparatus for in situ nanoparticle monitoring during flame assisted synthesis
- 1 October 2013
- Published by Elsevier in Combustion and Flame
- Vol. 160 (10) , 2131-2140
Combined particle mass spectrometer – Quartz crystal microbalance apparatus for in situ nanoparticle monitoring during flame assisted synthesis
- 15 October 2001
- Published by Royal Society of Chemistry (RSC) in Faraday Discussions
- Vol. 119 (1) , 321-335
Laser absorption spectroscopy diagnostics of nitrogen-containing radicals in low-pressure hydrocarbon flames doped with nitrogen oxides
Absolute concentration profiles of NH2 and HNO have been measured in low-pressure methane/air flat flames doped with small amounts of NO and N2O. Addition of a small amount of nitrogen oxides does not alter significantly the flame speeds, temperature profiles and other parameters of the relatively well-understood methane/air flames. Intracavity laser absorption spectroscopy (ICLAS) and cavity ring-down spectroscopy (CRDS) are high-sensitivity techniques used to measure absolute concentrations of minor species in flames. In this work ICLAS is used to monitor NH2 and HNO, whereas CRDS is used for temperature measurements using OH spectra in the UV range. The (090)–(000) and (080)–(000) bands of the Ã2A1– 2B1 electronic transition of NH2 and (100)–(000) and (011)–(000) bands of the Ã1A″– 1A′ transition of HNO are used. Methane flames of different equivalence ratios are used. NH2 and HNO are observed in the flame as well as in the zone surrounding the flame, closer to the walls of the low-pressure chamber where the burner is located. An absorption originating from the species in this zone can affect substantially the results of line-of-sight experiments. A slow flow of nitrogen through the optical window holders was added in order to separate the spectra of HNO originating from the central flame zone. Calculations based on the commonly used GRI-Mech chemical mechanism predict two maxima in the HNO concentration profile in the NO doped flames. The first is located in the vicinity of the burner, and the second is closer to the luminescence flame zone. We were able to observe the first maximum, and its measured location agrees well with prediction. On the other hand, GRI-Mech strongly underpredicts the observed absolute concentration of HNO in this maximum. The measured absolute concentrations of NH2 are in reasonable agreement with the GRI-Mech predictions.
- 15 October 2001
- Published by Royal Society of Chemistry (RSC) in Faraday Discussions
- Vol. 119 (1) , 321-335
Laser absorption spectroscopy diagnostics of nitrogen-containing radicals in low-pressure hydrocarbon flames doped with nitrogen oxides
Absolute concentration profiles of NH2 and HNO have been measured in low-pressure methane/air flat flames doped with small amounts of NO and N2O. Addition of a small amount of nitrogen oxides does not alter significantly the flame speeds, temperature profiles and other parameters of the relatively well-understood methane/air flames. Intracavity laser absorption spectroscopy (ICLAS) and cavity ring-down spectroscopy (CRDS) are high-sensitivity techniques used to measure absolute concentrations of minor species in flames. In this work ICLAS is used to monitor NH2 and HNO, whereas CRDS is used for temperature measurements using OH spectra in the UV range. The (090)–(000) and (080)–(000) bands of the Ã2A1– 2B1 electronic transition of NH2 and (100)–(000) and (011)–(000) bands of the Ã1A″– 1A′ transition of HNO are used. Methane flames of different equivalence ratios are used. NH2 and HNO are observed in the flame as well as in the zone surrounding the flame, closer to the walls of the low-pressure chamber where the burner is located. An absorption originating from the species in this zone can affect substantially the results of line-of-sight experiments. A slow flow of nitrogen through the optical window holders was added in order to separate the spectra of HNO originating from the central flame zone. Calculations based on the commonly used GRI-Mech chemical mechanism predict two maxima in the HNO concentration profile in the NO doped flames. The first is located in the vicinity of the burner, and the second is closer to the luminescence flame zone. We were able to observe the first maximum, and its measured location agrees well with prediction. On the other hand, GRI-Mech strongly underpredicts the observed absolute concentration of HNO in this maximum. The measured absolute concentrations of NH2 are in reasonable agreement with the GRI-Mech predictions.
- 22 May 1997
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 106 (20) , 8384-8391
Absolute HCO concentration measurements in methane/air flame using intracavity laser spectroscopy
Intracavity laser absorption spectroscopy was used to measure the absorption spectra of a premixed, flat methane/air flame at a total pressure of 30 Torr. The spectra were measured in the spectral range of A flat flame burner was placed inside the cavity of a broadband dye laser pumped by a cw argon-ion laser. The spectrum of the laser output was measured by a high resolution spectrograph (with a spectral resolution of 0.003 nm). The spectrum of HCO radicals transition) was measured with a high signal-to-noise ratio at different positions above the burner, providing the first quantitative measurement of the absolute concentrations of the HCO radical in flames. The linewidths of the individual rotational lines in the spectrum can be closely fitted by the equation where and The rotational temperature of the HCO radicals was evaluated from the spectra, but the error and the data scatter are relatively high since the lines with a high rotational quantum number are strongly superimposed with lines from different branches. The “hot band,” which can be assigned to the transition (0,0,1)–(0,9,1), was observed in spectra measured at high temperature. The value is evaluated from the position of this “hot band.” The concentration profile of the HCO radical has a maximum value of about which is in reasonable agreement with computer simulation results, when the uncertainties of the absorption cross section and of the rate constants for HCO reactions are taken into account. The relatively strong lines of the radical spectrum (the transition) were also recorded in the studied wavelength range. The spectra of these two radicals can be measured simultaneously which is advantageous in combustion diagnostics.- 22 May 1997
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 106 (20) , 8384-8391
Absolute HCO concentration measurements in methane/air flame using intracavity laser spectroscopy
Intracavity laser absorption spectroscopy was used to measure the absorption spectra of a premixed, flat methane/air flame at a total pressure of 30 Torr. The spectra were measured in the spectral range of A flat flame burner was placed inside the cavity of a broadband dye laser pumped by a cw argon-ion laser. The spectrum of the laser output was measured by a high resolution spectrograph (with a spectral resolution of 0.003 nm). The spectrum of HCO radicals transition) was measured with a high signal-to-noise ratio at different positions above the burner, providing the first quantitative measurement of the absolute concentrations of the HCO radical in flames. The linewidths of the individual rotational lines in the spectrum can be closely fitted by the equation where and The rotational temperature of the HCO radicals was evaluated from the spectra, but the error and the data scatter are relatively high since the lines with a high rotational quantum number are strongly superimposed with lines from different branches. The “hot band,” which can be assigned to the transition (0,0,1)–(0,9,1), was observed in spectra measured at high temperature. The value is evaluated from the position of this “hot band.” The concentration profile of the HCO radical has a maximum value of about which is in reasonable agreement with computer simulation results, when the uncertainties of the absorption cross section and of the rate constants for HCO reactions are taken into account. The relatively strong lines of the radical spectrum (the transition) were also recorded in the studied wavelength range. The spectra of these two radicals can be measured simultaneously which is advantageous in combustion diagnostics.- 1 March 1995
- Published by Elsevier in Combustion and Flame
- Vol. 100 (4) , 550-558
Mechanism of sulfur chemiluminescent emission in pulsed flames
- 1 March 1995
- Published by Elsevier in Combustion and Flame
- Vol. 100 (4) , 550-558
Mechanism of sulfur chemiluminescent emission in pulsed flames